CAS 67878-76-6

methyl 5-bromonaphthalene-2-carboxylate

Description:

Methyl 5-bromonaphthalene-2-carboxylate is an organic compound characterized by its structure, which includes a naphthalene ring substituted with a bromine atom and a carboxylate ester functional group. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its aromatic properties, which contribute to its stability and reactivity. The presence of the bromine atom enhances its electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions and coupling reactions. Methyl 5-bromonaphthalene-2-carboxylate is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It is important to handle this compound with care, as it may pose health risks if inhaled or ingested, and appropriate safety measures should be taken during its use in laboratory settings. Additionally, its solubility in organic solvents makes it suitable for various applications in chemical research and industry.

Formula: C₁₂H₉BrO₂

InChI: InChI=1/C12H9BrO2/c1-15-12(14)9-5-6-10-8(7-9)3-2-4-11(10)13/h2-7H,1H3

SMILES: COC(=O)c1ccc2c(cccc2Br)c1

Synonyms:

• 2-Naphthalenecarboxylic Acid, 5-Bromo-, Methyl Ester
• Methyl 5-bromo-2-naphthoate
• Methyl-5-bromnaphthalen-2-carboxylat

Methyl 5-bromo-2-naphthoate

CAS: 67878-76-6

Formula: C₁₂H₉BrO₂

Purity: 98%

Color and Shape: Solid

Molecular weight: 265.1027

Ref: IN-DA00FBQV

Methyl 5-bromo-2-naphthoate

CAS: 67878-76-6

Methyl 5-bromo-2-naphthoate

Purity: 98%

Molecular weight: 265.10g/mol

Ref: 54-OR77614

Methyl 5-bromo-2-naphthoate

CAS: 67878-76-6

Formula: C₁₂H₉BrO₂

Purity: 98%

Color and Shape: Liquid, No data available.

Molecular weight: 265.106

Ref: 10-F511412

Methyl 5-bromo-2-naphthoate

CAS: 67878-76-6

Methyl 5-bromo-2-naphthoate is a Grignard reagent that reacts with a variety of organic compounds. It has been used in the synthesis of polymers, such as polyvinyl chloride, and yields higher yields than other Grignard reagents. Methyl 5-bromo-2-naphthoate can also be used to synthesize butyllithium, which is an organolithium compound that is commonly used as a strong base in organic synthesis. This reagent can be prepared by reacting magnesium with chloroform and bromine. Methyl 5-bromo-2-naphthoate also reacts with acetylene to form ethynyl bromide. The elimination reactions between methyl 5-bromo-2-naphthoate and hydrogen halides produce trifluoromethyl bromide or trifluoromethyl iodide.

Formula: C₁₂H₉BrO₂

Purity: Min. 95%

Molecular weight: 265.1 g/mol

Ref: 3D-SCA87876